rs863224059
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GG;GG) | 0 | common in clinvar |
Make rs863224059(GG;TTT) |
Make rs863224059(TTT;TTT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 43957384 |
Gene | LRPPRC |
is a | snp |
is | mentioned by |
dbSNP | rs863224059 |
dbSNP (classic) | rs863224059 |
ClinGen | rs863224059 |
ebi | rs863224059 |
HLI | rs863224059 |
Exac | rs863224059 |
Gnomad | rs863224059 |
Varsome | rs863224059 |
LitVar | rs863224059 |
Map | rs863224059 |
PheGenI | rs863224059 |
Biobank | rs863224059 |
1000 genomes | rs863224059 |
hgdp | rs863224059 |
ensembl | rs863224059 |
geneview | rs863224059 |
scholar | rs863224059 |
rs863224059 | |
pharmgkb | rs863224059 |
gwascentral | rs863224059 |
openSNP | rs863224059 |
23andMe | rs863224059 |
SNPshot | rs863224059 |
SNPdbe | rs863224059 |
MSV3d | rs863224059 |
GWAS Ctlg | rs863224059 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224059(TTT;TTT) |
Alt | rs863224059(TTT;TTT) |
Reference | Rs863224059(GG;GG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | LRPPRC |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.44184523_44184524delCCinsAAA |
CLNSRC | |
CLNACC | RCV000196368.1, |